Abstract
1. Active frog sartorius muscle in vitro liberates a substance into the bathing solution which has a pronounced stimulatory action on the frog heart.
2. The stimulatory effect is not due to an increase in the K+ concentration of the bathing solution, nor is it due to the liberation of catecholamines.
3. In a molecular sieve chromatography procedure the stimulatory substance can be eluted in a single fraction which shows a maximum absorption of U.V. light at a wave-length of 265 nm, indicative of the presence of substances containing a purine ring.
4. Low concentrations (10-7-10-8 g/ml.) of adenosine triphosphate (ATP), adenosine diphosphate (ADP) and uridine triphosphate (UTP) have a marked stimulatory action on the frog heart. The action of ATP and ADP on the heart is qualitatively very similar to that of the muscle bathing solution, while the action of UTP is distinctly different. The triphosphates of inosine, cytidine and guanosine stimulate the heart when in high concentration only. Adenosine and adenosine monophosphate do not stimulate the heart.
5. Incubation of the muscle bathing solution and of solutions of ATP with the enzyme apyrase for the same time produces a similar marked reduction in the stimulatory action of both on the heart. Apyrase catalyses the break-down of nucleotide triphosphates to monophosphates.
6. The elution behaviour of the stimulatory substance determined by molecular sieve chromatography is the same as that for ATP.
7. The muscle bathing solution causes light to be emitted from firefly lantern extract, the pattern of light emission being similar to that produced by nucleotide triphosphates.
8. The concentrations of ATP having the same quantitative action on the frog heart and on firefly extract as a given muscle bathing solution are almost identical, whereas the matching concentrations of ADP and UTP in the two methods of assay are widely different.
9. It is concluded that ATP is released from active frog skeletal muscle in vitro. This release may play an important part in the reactive hyperaemia of muscular exercise since ATP has a powerful vasodilator action.
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Selected References
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- BOYD I. A., PATHAK C. L. THE RESPONSE OF PERFUSED FROG HEARTS TO MINUTE QUANTITIES OF ACETYLCHOLINE, AND THE VARIATION IN SENSITIVITY WITH SEASON. J Physiol. 1965 Jan;176:191–204. doi: 10.1113/jphysiol.1965.sp007544. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DYDYNSKA M., WILKIE D. R. THE OSMOTIC PROPERTIES OF STRIATED MUSCLE FIBERS IN HYPERTONIC SOLUTIONS. J Physiol. 1963 Nov;169:312–329. doi: 10.1113/jphysiol.1963.sp007258. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Drury A. N., Szent-Györgyi A. The physiological activity of adenine compounds with especial reference to their action upon the mammalian heart. J Physiol. 1929 Nov 25;68(3):213–237. doi: 10.1113/jphysiol.1929.sp002608. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Endo M. Entry of fluorescent dyes into the sarcotubular system of the frog muscle. J Physiol. 1966 Jul;185(1):224–238. doi: 10.1113/jphysiol.1966.sp007983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Forrester T. Release of adenosine triphosphate from active skeletal muscle. J Physiol. 1966 Oct;186(2):107P–109P. [PubMed] [Google Scholar]
- Glick D. Histochemical Localization of Adenosinetriphosphatase. Science. 1946 May 10;103(2680):599–599. doi: 10.1126/science.103.2680.599-a. [DOI] [PubMed] [Google Scholar]
- HILL D. K. Autoradiographic localization of adenine nucleotide in frog's striated muscle. J Physiol. 1959 Jan 28;145(1):132–174. doi: 10.1113/jphysiol.1959.sp006133. [DOI] [PMC free article] [PubMed] [Google Scholar]
- HUXLEY H. E. EVIDENCE FOR CONTINUITY BETWEEN THE CENTRAL ELEMENTS OF THE TRIADS AND EXTRACELLULAR SPACE IN FROG SARTORIUS MUSCLE. Nature. 1964 Jun 13;202:1067–1071. doi: 10.1038/2021067b0. [DOI] [PubMed] [Google Scholar]
- LIEBECQ C., LALLEMAND A., DEGUELDRE-GUILLAUME M. J. [Partial purification and properties of potato apyrase]. Bull Soc Chim Biol (Paris) 1963;45:573–594. [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- McElroy W. D. The Energy Source for Bioluminescence in an Isolated System. Proc Natl Acad Sci U S A. 1947 Nov;33(11):342–345. doi: 10.1073/pnas.33.11.342. [DOI] [PMC free article] [PubMed] [Google Scholar]
- TRAVERSO-CORI A., CORI O. Splitting of the terminal phosphate group of adenosine triphosphate by potato apyrase. Biochim Biophys Acta. 1962 Feb 12;57:158–160. doi: 10.1016/0006-3002(62)91096-x. [DOI] [PubMed] [Google Scholar]
- VERSPRILLE A. THE INITAL PHASE OF THE POSITIVE INOTROPIC EFFECT OF ATP ON THE ISOLATED FROG HEART. Pflugers Arch Gesamte Physiol Menschen Tiere. 1963;277:684–687. doi: 10.1007/BF00363286. [DOI] [PubMed] [Google Scholar]
- WILKINSON R. H. A micro-method for serum calcium and serum magnesium. J Clin Pathol. 1957 May;10(2):126–135. doi: 10.1136/jcp.10.2.126. [DOI] [PMC free article] [PubMed] [Google Scholar]